JP2017518401A - 樹脂用ポリエステル系可塑剤 - Google Patents
樹脂用ポリエステル系可塑剤 Download PDFInfo
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- JP2017518401A JP2017518401A JP2016564263A JP2016564263A JP2017518401A JP 2017518401 A JP2017518401 A JP 2017518401A JP 2016564263 A JP2016564263 A JP 2016564263A JP 2016564263 A JP2016564263 A JP 2016564263A JP 2017518401 A JP2017518401 A JP 2017518401A
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- Prior art keywords
- plasticizer
- resin
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- polyester plasticizer
- polyester
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- 239000004014 plasticizer Substances 0.000 title claims abstract description 68
- 229920000728 polyester Polymers 0.000 title claims abstract description 41
- 229920005989 resin Polymers 0.000 title claims abstract description 38
- 239000011347 resin Substances 0.000 title claims abstract description 38
- 239000000126 substance Substances 0.000 claims abstract description 14
- 239000004626 polylactic acid Substances 0.000 claims description 28
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 27
- -1 polybutylene succinate Polymers 0.000 claims description 13
- 229920001432 poly(L-lactide) Polymers 0.000 claims description 8
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 8
- 239000004800 polyvinyl chloride Substances 0.000 claims description 8
- JVTAAEKCZFNVCJ-REOHCLBHSA-N L-lactic acid Chemical compound C[C@H](O)C(O)=O JVTAAEKCZFNVCJ-REOHCLBHSA-N 0.000 claims description 6
- 229920006167 biodegradable resin Polymers 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 4
- 125000001033 ether group Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 229920000954 Polyglycolide Polymers 0.000 claims description 3
- 229920001610 polycaprolactone Polymers 0.000 claims description 3
- 239000004632 polycaprolactone Substances 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 239000004633 polyglycolic acid Substances 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- RBMHUYBJIYNRLY-UHFFFAOYSA-N 2-[(1-carboxy-1-hydroxyethyl)-hydroxyphosphoryl]-2-hydroxypropanoic acid Chemical compound OC(=O)C(O)(C)P(O)(=O)C(C)(O)C(O)=O RBMHUYBJIYNRLY-UHFFFAOYSA-N 0.000 claims 1
- 229920001434 poly(D-lactide) Polymers 0.000 claims 1
- 229920002961 polybutylene succinate Polymers 0.000 claims 1
- 239000004631 polybutylene succinate Substances 0.000 claims 1
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 22
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 12
- 238000005886 esterification reaction Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- HWXBTNAVRSUOJR-UHFFFAOYSA-N alpha-hydroxyglutaric acid Natural products OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 description 11
- 229940009533 alpha-ketoglutaric acid Drugs 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000001361 adipic acid Substances 0.000 description 8
- 235000011037 adipic acid Nutrition 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000002952 polymeric resin Substances 0.000 description 8
- 229920003002 synthetic resin Polymers 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 238000004817 gas chromatography Methods 0.000 description 5
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- 239000005556 hormone Substances 0.000 description 4
- 229940088597 hormone Drugs 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- 229920002988 biodegradable polymer Polymers 0.000 description 3
- 239000004621 biodegradable polymer Substances 0.000 description 3
- 239000004790 ingeo Substances 0.000 description 3
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UWTATZPHSA-N D-lactic acid Chemical compound C[C@@H](O)C(O)=O JVTAAEKCZFNVCJ-UWTATZPHSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229940022769 d- lactic acid Drugs 0.000 description 2
- 238000006481 deamination reaction Methods 0.000 description 2
- 229930195712 glutamate Natural products 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000008029 phthalate plasticizer Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- KPGXRSRHYNQIFN-UHFFFAOYSA-L 2-oxoglutarate(2-) Chemical compound [O-]C(=O)CCC(=O)C([O-])=O KPGXRSRHYNQIFN-UHFFFAOYSA-L 0.000 description 1
- JJTUDXZGHPGLLC-IMJSIDKUSA-N 4511-42-6 Chemical compound C[C@@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-IMJSIDKUSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 239000000817 Petroleum-derived resin Substances 0.000 description 1
- 238000005537 brownian motion Methods 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0016—Plasticisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/716—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/018—Additives for biodegradable polymeric composition
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Biological Depolymerization Polymers (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
Rは、線状または分枝状のC2−C20アルキレンであり、アルキレンの炭素鎖中間に、酸素をエーテル構造として0個以上含み、
mは、1ないし20の整数である。
Rは、線状または分枝状のC2−C20アルキレンであり、アルキレンの炭素鎖中間に、酸素をエーテル構造として0個以上含み、
mは、1ないし20の整数である。
Rは、線状または分枝状のC2−C20アルキレンであり、アルキレンの炭素鎖中間に、酸素をエーテル構造として0個以上含み、
mは、1ないし20の整数である。
アルファ−ケトグルタル酸(55.9重量%)、1,3−プロパンジオール(36.1重量%)、及び下記組成の混合アルコール(7.3重量%)を、コンデンサを装着したフラスコに入れて徐々に昇温させ、170−210℃範囲で撹拌すると共に温度を維持させて還流し、エステル化(esterification)反応を進めた。
得られたポリエステル分子量Mn:1893(GPC)、酸価:16.5(mg、KOH)
アルファ−ケトグルタル酸(55.1重量%)、1,2−プロパンジオール(37.5重量%)、及び下記組成の混合アルコール(7.5重量%)を、コンデンサを装着したフラスコに入れて徐々に昇温させ、170−210℃範囲で撹拌すると共に温度を維持させて還流し、エステル化反応を進めた。
混合アルコール:ガスクロマトグラフィでの測定時、C6(hexyl)1−2%、C8(caprylic)40−42%、C10(decyl)54−57%、C12(lauryl)最大1.0%、炭化水素最大1.0%
アルファ−ケトグルタル酸(56.2重量%)、1,2−プロパンジオール(35.7重量%)、及び下記組成の混合アルコール(7.2重量%)を、コンデンサを装着したフラスコに入れて徐々に昇温させ、170−210℃範囲で撹拌すると共に温度を維持させて還流し、エステル化反応を進めた。
アジピン酸を単量体として含むポリエステル可塑剤を製造した。アジピン酸(57.5重量%)、1,3−プロパンジオール(34。2重量%)、及び下記組成の混合アルコール(7.1重量%)を、コンデンサを装着したフラスコに入れて徐々に昇温させ、170−210℃範囲で撹拌すると共に温度を維持させて還流し、エステル化反応を進めた。
生分解性樹脂であるNatureWorks LLC社のポリ乳酸常用製品であるINGEO2003Dに可塑剤を使用しない。
一般的に使用されるアジピン酸を単量体にして、ポリエステル可塑剤を製造した。アジピン酸(57.1重量%)、1,3−プロパンジオール(34.3重量%)、及び下記組成の混合アルコール(7.2重量%)を、コンデンサを装着したフラスコに入れて徐々に昇温させ、170−210℃範囲で撹拌すると共に温度を維持させて還流し、エステル化反応を進めた。
汎用性樹脂であるTaiyo vinyl社のPVC常用製品TH−1000に可塑剤を使用しない。
前記実施例1−3、及び比較例1−4で製造されたサンプルに対して、ガラス転移温度Tg及び縁融点Tmの熱的特性を、DSC ASTM D3418、10℃/min方法によって測定した。
Claims (4)
- 前記ポリエステル系可塑剤は、ポリ乳酸(PLLA、PDLA)、sc−PLA(stereocomplex−PLA))、ポリカプロラクトン、ポリグリコール酸、ポリカーボネート及びポリブチレンスクシネートから構成された群のうちから選択された1以上の生分解性樹脂に適用されることを特徴とする請求項1または2に記載のポリエステル系可塑剤。
- 前記ポリエステル系可塑剤は、ポリ塩化ビニル、ポリエチレン、ポリプロピレン、アクリロニトリル−ブタジエン−スチレン樹脂(ABS樹脂)及びポリスチレンから構成された群のうちから選択された1以上の汎用性樹脂に適用されることを特徴とする請求項1または2に記載のポリエステル系可塑剤。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2014-0049555 | 2014-04-24 | ||
KR20140049555 | 2014-04-24 | ||
PCT/KR2015/002599 WO2015163582A2 (ko) | 2014-04-24 | 2015-03-18 | 수지용 폴리에스테르계 가소제 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2017518401A true JP2017518401A (ja) | 2017-07-06 |
JP6486963B2 JP6486963B2 (ja) | 2019-03-20 |
Family
ID=54333386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016564263A Active JP6486963B2 (ja) | 2014-04-24 | 2015-03-18 | 樹脂用ポリエステル系可塑剤 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9725574B2 (ja) |
EP (1) | EP3135721A4 (ja) |
JP (1) | JP6486963B2 (ja) |
KR (1) | KR101741697B1 (ja) |
CN (1) | CN107108959B (ja) |
WO (1) | WO2015163582A2 (ja) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11427688B2 (en) * | 2017-04-17 | 2022-08-30 | Eastman Chemical Company | Copolyesters plasticized with polymeric plasticizer |
US20220226499A1 (en) * | 2019-05-16 | 2022-07-21 | Arizona Board Of Regents On Behalf Of Arizona State University | Metabolite Delivery for Modulating Metabolic Pathways of Cells |
WO2021142254A1 (en) * | 2020-01-08 | 2021-07-15 | Abhinav Acharya | Metabolite-based polymers, microparticles, and nanoparticles for immunotherapy and methods of treating a disease or disorder |
EP3992227A1 (en) | 2020-07-20 | 2022-05-04 | Bio Bond ApS | Bio-based plasticiser for resins and blends containing said plasticiser |
DE102020124314A1 (de) * | 2020-09-17 | 2022-03-17 | Heinrich-Heine-Universität Düsseldorf | Biologisch abbaubare Klebstoff-Zusammensetzung |
CN115785595A (zh) * | 2022-11-28 | 2023-03-14 | 河源市普立隆新材料科技有限公司 | 一种基于无水增塑的聚乙烯醇熔融吹塑薄膜及其制备方法 |
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2015
- 2015-03-18 CN CN201580021992.9A patent/CN107108959B/zh active Active
- 2015-03-18 EP EP15783628.9A patent/EP3135721A4/en not_active Withdrawn
- 2015-03-18 JP JP2016564263A patent/JP6486963B2/ja active Active
- 2015-03-18 US US15/305,862 patent/US9725574B2/en active Active
- 2015-03-18 WO PCT/KR2015/002599 patent/WO2015163582A2/ko active Application Filing
- 2015-03-19 KR KR1020150038316A patent/KR101741697B1/ko active IP Right Grant
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US4398019A (en) * | 1980-11-07 | 1983-08-09 | Imperial Chemical Industries Plc | Anisotropic melt forming polyesters and polyesteramides |
JPH01104264A (ja) * | 1987-10-19 | 1989-04-21 | Terumo Corp | 医療用軟質樹脂組成物および医療用具 |
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Also Published As
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EP3135721A2 (en) | 2017-03-01 |
WO2015163582A3 (ko) | 2017-06-22 |
CN107108959B (zh) | 2019-10-25 |
KR101741697B1 (ko) | 2017-05-31 |
JP6486963B2 (ja) | 2019-03-20 |
US9725574B2 (en) | 2017-08-08 |
WO2015163582A2 (ko) | 2015-10-29 |
CN107108959A (zh) | 2017-08-29 |
US20170066901A1 (en) | 2017-03-09 |
EP3135721A4 (en) | 2018-07-11 |
KR20150123153A (ko) | 2015-11-03 |
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